Neuropathy and constipation
I've always had issues with constipation. I've got SFN now for 2 years in my feet and hands, numbness mainly, and notice my constipation is getting worse. Any suggestions?
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Unfortunately taking more fiber with a non working colon only leads to a backup in the colon. The muscles that are supposed to get the colon to move the food along aren't working and so it sits there and compacts and loses moisture content and hardens. I have been taking a generic form of Miralax and at least it keeps it from hardening but it doesn't move any faster.
Yes, I have had a full workup with my gastroenterologist. I had a defacography, which is an x-ray of bowel function. Not a pleasant test, but it revealed a sluggish colon which does not function properly. My gastroenterologist basically said that my neuropathy was causing the problem with elimination and that I would probably have to rely on suppositories and enemas. Bulck and fibre just backs up. Miralax helps some but my colon is still sluggish and does not form proper stool.
Did your spine surgery help at all with neuropathy, balance, standing and walking. Right now I can no walk safely without my walker, standing in shower for more than a few minutes leaves me wobbly . Standing to cook for only 5 to 10 minutes results in icey tingling and weakness in legs. If you had any of these symptoms did the surgery help?
I too was recommended senicot for constipation due to taking Cymbalta. I have strained and caused a hiatal hernia. It was recommended to take senicot twice a day. I'm playing around with the dosage as I think twice a day would be too much. I find senicot gives me a normal bowel movement. My husband takes Miralax daily. It helps him. I know Miralax is a safe laxative as it was given to newborn premies daily. If it's safe for those babies, it must be safe for adults to take daily too. When they were alive, my aging parents were told to take Miralax daily.
My primary doc says taking a daily mild laxative is ok in aging adults. If we were 25, he might have concerns. Check with your primary doc. He's probably has lots of experience with older adults and constipation.
Good luck,
vlpr
Yes. But what really made a difference was a lot of PT and now I am going to a special gym working on my legs and back strength. It took at least a year before I was somewhat comfortable around the house but still using a cane and still not perfect with balance. It is 2 years now since my spine surgery and I still have to be careful with my balance.
Thanks for info John. I’m having terrible constipation and took Miralax 2 days ago to no avail. I’ve taken aloe Vera juice as well. Does miralax take awhile to help?
Miralax normally works overnight but sometimes has been hit or miss for me and I've had to use 1-1/2 to 2 capfuls. I've also found Magnesium Citrate liquid solution to help when I'm really having a terrible bout of constipation but I absolutely hate the sweet taste 😝. My favorite aid is a night time cup of hot Prunelax tea (https://www.amazon.com/dp/B07DFSNYQW).
I've been experimenting the past 2 months and found that Heather's Tummy Fiber is helping with my bowel regularity but I haven't quite got it down to how much/little I need to use daily for my constipation. It can be used for both diarrhea and constipation. The only downside from my perspective is it takes a little more effort to mix it up with water as it doesn't mix well with hot or cold liquids. Works great in smoothies or mixed with food. - https://www.heatherstummycare.com/c/tummy-fiber/. I also like their Peppermint & Fennel tea bags which help with bloating/gas.
I would go with something stronger when this occurs, like a laxative pill that induces actual bowel cramping. It’s not fun, but you can use it to get back on track, then play around with something milder for daily use if needed.
Someone here mentioned Colon Max (Amazon). Okay, this works! I am also on prescription Motegrity every morning. This didn’t happen overnight - looking back, I realize I was starting to struggle with some bloating and slow gut motility long before all my SFN pain began. For years. This is what works currently for me, and sometimes even this doesn’t work. Those nerves just aren’t working properly, it’s just a fact, like other in-fun SFN realities.
Thank you for all the suggestions as I have similar problem.